{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Little Rock",
      "state": "AR",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72028",
      "recalling_firm": "Cantrell Drug Company",
      "address_1": "7321 Cantrell Rd",
      "address_2": "N/A",
      "postal_code": "72207-4144",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1153-2016",
      "product_description": "Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL),  in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453",
      "product_quantity": "a) 450 syringes and b) 1250 syringes",
      "reason_for_recall": "Subpotent Drug",
      "recall_initiation_date": "20150821",
      "center_classification_date": "20160706",
      "termination_date": "20170203",
      "report_date": "20160713",
      "code_info": "a) Lots: 149690, exp 9/14/15 and 151665, exp 11/5/15 and   b) Lots: 149198, exp 9/3/15; 151454, exp 9/14/15; 151668, exp 11/5/15 and 151962, exp 11/11/15"
    }
  ]
}